Resorbable Magnesium Scaffolds Registry

Biotronik

Status: Enrolling

Conditions: Coronary Artery Disease

Treatments: Device: Freesolve; Device: Magmaris

Study type: Observational

Funder types: Industry

Identifiers

NCT04679740

C1908

Details and patient eligibility

About

The registry follows the ESC/EACTS guideline and further investigates the clinical performance and short-term safety of RMS (Resorbable Magnesium Scaffolds) in a real world setting within the scope of its intended use without further (medical related) exclusion criteria according to their respective instructions for use (IFU).

Enrollment: 1,106 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• According to the IFU

Exclusion criteria

• According to the IFU